Temporary Clinical Research Associate
Core
Conduct remote and onsite monitoring activities for clinical research studies to ensure protocol adherence, data accuracy, and regulatory compliance.
Role type
Temporary Clinical Research Associate (CRA)
Builds
Clinical research studies for WHOOP's health and performance monitoring products
Domain
Clinical research / Digital health / Wearable technology
Deliverable
client delivery
Required skills
Clinical monitoring, protocol adherence, GCP compliance, source data verification, risk identification, study documentation, site readiness support, regulatory knowledge
Preferred skills
Medical device study experience, ISO 14155 familiarity, sponsor/CRO/site environment experience, cardiovascular/women's health/digital biomarkers domain knowledge
Technologies
Clinical research systems, monitoring templates, study logs
Responsibilities
Conduct remote and onsite monitoring visits (SIV, interim, closeout); Review informed consent, eligibility, source docs, CRFs, and safety data; Prepare monitoring reports and action trackers; Identify and escalate protocol deviations and compliance risks; Support site readiness and team training; Assist with study closeout and Trial Master File completion
Seniority
Mid-level, hands-on IC